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Gene expression during cartilage differentiation in turkey tibial dyschondroplasia, evaluated by in situ hybridization
Year:
1997
Source of publication :
Avian Diseases
Authors :
Hurvitz, Shmuel (Animal science)
;
.
Knopov, Viktor
;
.
Pines, Mark
;
.
Volume :
41
Co-Authors:
Knopov, V., Institute of Animal Science, Agricultural Research Organization, Volcani Center, Bet Dagan 50250, Israel
Hadash, D., Avian Disease Laboratory, Raananah, Israel
Hurwitz, S., Institute of Animal Science, Agricultural Research Organization, Volcani Center, Bet Dagan 50250, Israel
Leach, R.M., Department of Poultry Sciences, Pennsylvania State University, University Park, PA 16802-3501, United States
Pines, M., Institute of Animal Science, Agricultural Research Organization, Volcani Center, Bet Dagan 50250, Israel
Facilitators :
From page:
62
To page:
72
(
Total pages:
11
)
Abstract:
Gene expression and alkaline phosphatase (AP) activity, associated with chondrocyte differentiation, were evaluated in the epiphyses of normal and tibial dyschondroplasia (TD)-afflicted turkeys. In the normal turkey growth plate (GP), osteopontin (OPN) and type X collagen genes were expressed by the hypertrophic cells in both GP and secondary ossification center, parallel to manifestation of AP activity. Collagen type II gene expression was restricted to the nonhypertrophic chondrocytes at the upper part of the GP OPN or collagen type X genes were not expressed within the TD lesion. However, these genes were expressed in areas proximal and distal to the lesion, suggesting that after reaching partial differentiation, chondrocytes within the developing TD lesion de-differentiate into cells that resemble chondrocytes in the prehypertrophic zone. This suggestion is supported by the observation that the cells in the lesion expressed the collagen type II gene. In some cases, the TD lesion was invaded by fibroblastlike cells that did not exhibit any AP activity or express the OPN gene. No lesions were observed in the secondary ossification centers.
Note:
Related Files :
Animal
Animals
biosynthesis
Differentiation
gene expression
metabolism
Pathology
Phosphoproteins
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Related Content
More details
DOI :
Article number:
0
Affiliations:
Database:
Scopus
Publication Type:
article
;
.
Language:
English
Editors' remarks:
ID:
27605
Last updated date:
21/08/2022 07:45
Creation date:
17/04/2018 00:32
Scientific Publication
Gene expression during cartilage differentiation in turkey tibial dyschondroplasia, evaluated by in situ hybridization
41
Knopov, V., Institute of Animal Science, Agricultural Research Organization, Volcani Center, Bet Dagan 50250, Israel
Hadash, D., Avian Disease Laboratory, Raananah, Israel
Hurwitz, S., Institute of Animal Science, Agricultural Research Organization, Volcani Center, Bet Dagan 50250, Israel
Leach, R.M., Department of Poultry Sciences, Pennsylvania State University, University Park, PA 16802-3501, United States
Pines, M., Institute of Animal Science, Agricultural Research Organization, Volcani Center, Bet Dagan 50250, Israel
Gene expression during cartilage differentiation in turkey tibial dyschondroplasia, evaluated by in situ hybridization
Gene expression and alkaline phosphatase (AP) activity, associated with chondrocyte differentiation, were evaluated in the epiphyses of normal and tibial dyschondroplasia (TD)-afflicted turkeys. In the normal turkey growth plate (GP), osteopontin (OPN) and type X collagen genes were expressed by the hypertrophic cells in both GP and secondary ossification center, parallel to manifestation of AP activity. Collagen type II gene expression was restricted to the nonhypertrophic chondrocytes at the upper part of the GP OPN or collagen type X genes were not expressed within the TD lesion. However, these genes were expressed in areas proximal and distal to the lesion, suggesting that after reaching partial differentiation, chondrocytes within the developing TD lesion de-differentiate into cells that resemble chondrocytes in the prehypertrophic zone. This suggestion is supported by the observation that the cells in the lesion expressed the collagen type II gene. In some cases, the TD lesion was invaded by fibroblastlike cells that did not exhibit any AP activity or express the OPN gene. No lesions were observed in the secondary ossification centers.
Scientific Publication
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